scholarly journals Biological rational for sequential targeting of Bruton tyrosine kinase and Bcl-2 to overcome CD40-induced ABT-199 resistance in mantle cell lymphoma

Oncotarget ◽  
2015 ◽  
Vol 6 (11) ◽  
pp. 8750-8759 ◽  
Author(s):  
David Chiron ◽  
Christelle Dousset ◽  
Carole Brosseau ◽  
Cyrille Touzeau ◽  
Sophie Maïga ◽  
...  
2013 ◽  
Vol 37 (10) ◽  
pp. 1271-1277 ◽  
Author(s):  
Munevver Cinar ◽  
FaridSaei Hamedani ◽  
Zhicheng Mo ◽  
Bekir Cinar ◽  
Hesham M. Amin ◽  
...  

2020 ◽  
Author(s):  
Martin Dreyling ◽  
Constantine S Tam ◽  
Michael Wang ◽  
Stephen D Smith ◽  
Marco Ladetto ◽  
...  

Mantle cell lymphoma is an aggressive B-cell malignancy. Current frontline chemoimmunotherapies produce high response rates but relapse is inevitable. Furthermore, the elderly and those with comorbidities are precluded from standard regimens and stem cell transplant, leaving them with limited options. Targeted therapies, including Bruton tyrosine kinase inhibitors, are an effective treatment strategy in mantle cell lymphoma. Zanubrutinib is a potent next-generation Bruton tyrosine kinase inhibitor that has demonstrated complete and sustained Bruton tyrosine kinase occupancy, minimal off-target effects and favorable pharmacokinetic/pharmacodynamic properties. Described herein is an ongoing Phase III study comparing the efficacy and safety of zanubrutinib plus rituximab followed by zanubrutinib monotherapy versus bendamustine plus rituximab followed by observation in transplant-ineligible patients with previously untreated mantle cell lymphoma. Clinical Trial Registration: NCT04002297 ( ClinicalTrials.gov )


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